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Edwin M Stone

Showing results (191-200 of 384) with videos related to

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Stem Cell Research & Therapy|September 24, 2020
Stepwise differentiation and functional characterization of human induced pluripotent stem cell-derived choroidal endothelial cellsKelly Mulfaul, Joseph C Giacalone, Andrew P Voigt, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 3, 2004
Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assemblyKirk Mykytyn, Robert F Mullins, Michael Andrews, et al.
Ophthalmic Genetics|June 7, 2006
The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from IowaJohn H Fingert, Young H Kwon, Paula A Moore, et al.
Microvascular Research|December 21, 2018
Generation of an immortalized human choroid endothelial cell line (iChEC-1) using an endothelial cell specific promoterJoseph C Giacalone, Matthew J Miller, Grefachew Workalemahu, et al.
Plos One|January 4, 2017
Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1Doug D Chung, Ricardo F Frausto, Aleck E Cervantes, et al.
Investigative Ophthalmology & Visual Science|February 5, 2016
Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as ModifiersSuma P Shankar, Dianna K Hughbanks-Wheaton, David G Birch, et al.
Human Molecular Genetics|February 24, 2007
Glaucoma-causing myocilin mutants require the Peroxisomal targeting signal-1 receptor (PTS1R) to elevate intraocular pressureAllan R Shepard, Nasreen Jacobson, J Cameron Millar, et al.
Investigative Ophthalmology & Visual Science|March 26, 2005
A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)Izabela Sokal, William J Dupps, Michael A Grassi, et al.
The Journal of Pathology|November 14, 2015
Molecular response of chorioretinal endothelial cells to complement injury: implications for macular degenerationShemin Zeng, S Scott Whitmore, Elliott H Sohn, et al.
Investigative Ophthalmology & Visual Science|January 2, 2009
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Pageof 39

Showing results (191-200 of 384) with videos related to

Sort By:
Pageof 39
Stem Cell Research & Therapy|September 24, 2020
Stepwise differentiation and functional characterization of human induced pluripotent stem cell-derived choroidal endothelial cellsKelly Mulfaul, Joseph C Giacalone, Andrew P Voigt, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 3, 2004
Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assemblyKirk Mykytyn, Robert F Mullins, Michael Andrews, et al.
Ophthalmic Genetics|June 7, 2006
The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from IowaJohn H Fingert, Young H Kwon, Paula A Moore, et al.
Microvascular Research|December 21, 2018
Generation of an immortalized human choroid endothelial cell line (iChEC-1) using an endothelial cell specific promoterJoseph C Giacalone, Matthew J Miller, Grefachew Workalemahu, et al.
Plos One|January 4, 2017
Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1Doug D Chung, Ricardo F Frausto, Aleck E Cervantes, et al.
Investigative Ophthalmology & Visual Science|February 5, 2016
Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as ModifiersSuma P Shankar, Dianna K Hughbanks-Wheaton, David G Birch, et al.
Human Molecular Genetics|February 24, 2007
Glaucoma-causing myocilin mutants require the Peroxisomal targeting signal-1 receptor (PTS1R) to elevate intraocular pressureAllan R Shepard, Nasreen Jacobson, J Cameron Millar, et al.
Investigative Ophthalmology & Visual Science|March 26, 2005
A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)Izabela Sokal, William J Dupps, Michael A Grassi, et al.
The Journal of Pathology|November 14, 2015
Molecular response of chorioretinal endothelial cells to complement injury: implications for macular degenerationShemin Zeng, S Scott Whitmore, Elliott H Sohn, et al.
Investigative Ophthalmology & Visual Science|January 2, 2009
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Pageof 39